Biology – Quantitative Biology – Quantitative Methods
Scientific paper
2007-03-05
Proc. Natl. Acad. Sci. USA 103, 10907-10910 (2006)
Biology
Quantitative Biology
Quantitative Methods
The file contains: main text (+4 figures), supporting information (+9 figures), poster (1 page)
Scientific paper
10.1073/pnas.0604546103
The signal from many single molecule experiments monitoring molecular processes, such as enzyme turnover via fluorescence and opening and closing of ion channel via the flux of ions, consists of a time series of stochastic on and off (or open and closed) periods, termed a two-state trajectory. This signal reflects the dynamics in the underlying multi-substate on-off kinetic scheme (KS) of the process. The determination of the underlying KS is difficult and sometimes even impossible due to the loss of information in the mapping of the mutli dimensional KS onto two dimensions. Here we introduce a new procedure that efficiently and optimally relates the signal to all equivalent underlying KSs. This procedure partitions the space of KSs into canonical (unique) forms that can handle any KS, and obtains the topology and other details of the canonical form from the data without the need for fitting. Also established are relationships between the data and the topology of the canonical form to the on-off connectivity of a KS. The suggested canonical forms constitute a powerful tool in discriminating between KSs. Based on our approach, the upper bound on the information content in two state trajectories is determined.
Flomenbom Ophir
Silbey Robert J.
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